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CS-W001157 4
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Fmoc-Phe(3-CONH2)-OH

  • CAS No. 959573-22-9

  • Cat. No. CS-0137322
  • Purity≥97%
  • MDL No.MFCD06659144

*For research and further manufacturing use only, not for direct human use.

Fmoc-Phe(3-CONH2)-OH|CS-0137322

Structure of 959573-22-9

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General Information

  • CAS No. 959573-22-9
  • Cat. No. CS-0137322
  • Purity ≥97%
  • MDL No. MFCD06659144
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₂₂N₂O₅
  • Molecular Weight 430.45
  • Synonym(s) Fmoc-L-3-Carbamoylphe
  • SMILES O=C(O)[C@H](CC1=CC=CC(C(N)=O)=C1)NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O

Description

Fmoc-Phe(3-CONH2)-OH features a para-amino substituent on the phenyl ring, enhancing solubility and modulating electronic properties for optimized coupling efficiency. This derivative integrates seamlessly into peptide synthesis workflows, offering improved handling and reduced aggregation during chain elongation.

Application

Fmoc-Phe(3-CONH2)-OH serves as a key building block for the synthesis of peptide libraries and bioactive oligomers, featuring a meta-substituted phenylalanine derivative with a C-terminal amide. The Fmoc group enables efficient N-terminal protection in solid-phase peptide synthesis, while the 3-carboxamide functionality provides enhanced solubility and metabolic stability. This compound exhibits excellent bench stability, tolerates standard coupling conditions, and facilitates orthogonal functionalization in complex sequence assembly.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   118.72
  • LogP   3.3199
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   7

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